Department of Neurology, Samsung Medical Center, Seoul, Korea.
Neuroscience Center, Samsung Medical Center, Seoul, Korea.
Sci Rep. 2019 Nov 22;9(1):17329. doi: 10.1038/s41598-019-53980-y.
Clinically differentiating multiple system atrophy cerebellar (MSA-C) phenotype and spinocerebellar ataxias (SCAs) is challenging especially in the early stage. We assessed diagnostic value of brain magnetic resonance imaging (MRI) in differentiating MSA-C and SCAs based at different disease stages (<3, 3-7, and >7 years of disease duration). Overall, 186 patients with probable MSA-C and 117 with genetically confirmed SCAs were included. Hot cross bun (HCB) signs and middle cerebellar peduncle (MCP) hyperintensities were exclusively prevalent in MSA-C compared to SCAs at <3 years (HCB, 44.6% versus 0.9%; MCP hyperintensities, 38.3% versus 0.9%, respectively). Sensitivity, specificity, and positive predictive value (PPV) for HCB signs to differentiate MSA-C from SCAs were 45%, 99%, and 99% and those for MCP hyperintensities were 68%, 99%, and 99%, respectively; considering both HCB signs and MCP hyperintensities, specificity and PPV were 100%. However, the differential value of MRI signs decreased over time. MCP widths were smaller and showed more significant decrease in MSA-C than in SCAs. In conclusion, pontine and MCP changes were exclusively prominent in early stage MSA-C rather than in SCAs. Therefore, we should consider disease duration when interpreting pontine and MCP changes in brain MRIs, which will help better differentiate MSA-C and SCAs.
临床上区分多系统萎缩小脑型(MSA-C)表型和脊髓小脑共济失调(SCA)具有挑战性,尤其是在早期阶段。我们评估了脑磁共振成像(MRI)在区分不同疾病阶段(<3 年、3-7 年和>7 年)的 MSA-C 和 SCA 中的诊断价值。共有 186 例可能的 MSA-C 患者和 117 例遗传性 SCA 患者纳入研究。与 SCA 相比,在<3 年时,十字面包征(HCB)和小脑中脑脚(MCP)高信号仅在 MSA-C 中普遍存在(HCB:44.6%比 0.9%;MCP 高信号:38.3%比 0.9%)。HCB 征用于区分 MSA-C 和 SCA 的敏感性、特异性和阳性预测值(PPV)分别为 45%、99%和 99%,MCP 高信号的敏感性、特异性和 PPV 分别为 68%、99%和 99%;同时考虑 HCB 征和 MCP 高信号时,特异性和 PPV 为 100%。然而,MRI 征象的鉴别价值随时间推移而降低。MSA-C 的 MCP 宽度较小,且 MCP 宽度的减小更为显著。总之,在早期 MSA-C 中,桥脑和 MCP 的改变比 SCA 中更为突出。因此,在解释脑 MRI 中的桥脑和 MCP 改变时,我们应该考虑疾病持续时间,这将有助于更好地区分 MSA-C 和 SCA。